Evidence map›Paper›PMID 27654816›Full record

Trial reportPediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies2016

Dexmedetomidine Use in Critically Ill Children With Acute Respiratory Failure.

Mary Jo C Grant, James B Schneider, Lisa A Asaro, Brenda L Dodson, Brent A Hall, Shari L Simone, Allison S Cowl, Michele M Munkwitz, David Wypij, Martha A Q Curley and 1 more

2 registry-linked trialsAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00814099 nacompletednot on this map

Sedation Management in Pediatric Patients With Acute Respiratory Failure

TypeinterventionalSponsorUniversity of PennsylvaniaRan2009 to 2013Enrolled2,449ConditionsRespiratory Insufficiency, Respiratory Distress Syndrome, Newborn, Lung DiseasesArmsTeam approach to sedation management, Usual approach to sedation management
NCT03760978 completednot on this map

Efficacy and Safety of Dexmedetomidine for Prolonged Sedation in Pediatric Intensive Care Units

TypeobservationalSponsorAzienda Ospedaliera di PadovaRan2016 to 2018Enrolled163ConditionsProlonged SedationArmsDexmedetomidine
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

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  17. The Impact of a Clonidine Transition Protocol on Dexmedetomidine Withdrawal in Critically Ill Pediatric Patients.The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG · 2020
    Article
  18. Article
  19. Review
  20. [Application of dexmedetomidine in children with agitation during ventilator weaning].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2019
    Observational
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Mary Jo C Grant1Department of Pediatric Critical Care, Primary Children's Hospital, Salt Lake City, UT.2Division of Pediatric Critical Care Medicine, Cohen Children's Medical Center, Hofstra-Northwell School of Medicine, New York, NY.3Department of Cardiology, Boston Children's Hospital, Boston, MA.4Department of Pharmacy, Boston Children's Hospital, Boston, MA.5Department of Pharmacy, UC Davis Medical Center, Sacramento, CA.6Department of Pediatric Critical Care, University of Maryland Medical Center, Baltimore, MD.7Division of Pediatric Critical Care Medicine, Connecticut Children's Medical Center, Hartford, CT.8Division of Pediatric Critical Care Medicine, Department of Pediatric Critical Care, Phoenix Children's Hospital, University of Arizona College of Medicine, Phoenix, AZ.9Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA.10Department of Pediatrics, Harvard Medical School, Boston, MA.11Department of Family and Community Health, School of Nursing and Department of Anesthesia and Critical Care Medicine, the Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.12Department of Critical Care and Cardiovascular Nursing, Boston Children's Hospital, Boston, MA.
James B Schneider
Lisa A Asaro
Brenda L Dodson
Brent A Hall
Shari L Simone
Allison S Cowl
Michele M Munkwitz
David Wypij
Martha A Q Curley
Randomized Evaluation of Sedation Titration for Respiratory Failure Study Investigators
Boston Children's Hospital · USHarvard University · USUniversity of Maryland, Baltimore · US

Funding

Sedation Management in Pediatric Patients with Acute Respiratory FailureU01HL086622 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI CURLEY, MARTHA AQ · 2008 to 2013
$10.0M
Sedation Management in Pediatric Patients with Acute Respiratory Failure (DCC)U01HL086649 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI WYPIJ, DAVID · 2008 to 2012
$2.0M
NHLBI NIH HHS U01 HL086622NHLBI NIH HHS U01 HL086649
6 · The paper itself

Abstract

objectiveCare of critically ill children includes sedation but current therapies are suboptimal. To describe dexmedetomidine use in children supported on mechanical ventilation for acute respiratory failure.

designSecondary analysis of data from the Randomized Evaluation of Sedation Titration for Respiratory Failure clinical trial.

settingThirty-one PICUs. PATIENTS: Data from 2,449 children; 2 weeks to 17 years old.

interventionsSedation practices were unrestrained in the usual care arm. Patients were categorized as receiving dexmedetomidine as a primary sedative, secondary sedative, periextubation agent, or never prescribed. Dexmedetomidine exposure and sedation and clinical profiles are described. MEASUREMENTS AND MAIN

resultsOf 1,224 usual care patients, 596 (49%) received dexmedetomidine. Dexmedetomidine as a primary sedative patients (n = 138; 11%) were less critically ill (Pediatric Risk of Mortality III-12 score median, 6 [interquartile range, 3-11]) and when compared with all other cohorts, experienced more episodic agitation. In the intervention group, time in sedation target improved from 28% to 50% within 1 day of initiating dexmedetomidine as a primary sedative. Dexmedetomidine as a secondary sedative usual care patients (n = 280; 23%) included more children with severe pediatric acute respiratory distress syndrome or organ failure. Dexmedetomidine as a secondary sedative patients experienced more inadequate pain (22% vs 11%) and sedation (31% vs 16%) events. Dexmedetomidine as a periextubation agent patients (n = 178; 15%) were those known to not tolerate an awake, intubated state and experienced a shorter ventilator weaning process (2.1 vs 2.3 d).

conclusionsOur data support the use of dexmedetomidine as a primary agent in low criticality patients offering the benefit of rapid achievement of targeted sedation levels. Dexmedetomidine as a secondary agent does not appear to add benefit. The use of dexmedetomidine to facilitate extubation in children intolerant of an awake, intubated state may abbreviate ventilator weaning. These data support a broader armamentarium of pediatric critical care sedation.

Indexed as

Respiration, ArtificialAcute DiseaseAdolescentAirway ExtubationChildChild, PreschoolCritical CareCritical IllnessDexmedetomidineFemaleHumansHypnotics and SedativesInfantInfant, NewbornIntubation, IntratrachealMaleDexmedetomidineHypnotics and Sedatives

Identifiers

PMID27654816
PMCPMC5138139
OpenAlexW2523530926

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.